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HydroSil Go™ Intermittent Urinary Catheter 71808Recalls & reported problems

C. R. Bard, Inc. · HydroSil Go™ Intermittent Urinary Catheter · Class 2

All models of HydroSil Go Intermittent Urinary Catheter (6)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741097959), received between Sep 18, 2020 and Sep 18, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Damaged Prior to Receipt by User” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Device Damaged Prior to Receipt by User1
  • Manufacturing, Packaging or Shipping Problem1

Patient problems

  • No Known Impact Or Consequence To Patient1
  • No Patient Involvement1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 18, 2020Device Damaged Prior to Receipt by User; Manufacturing, Packaging or Shipping Problem; Device Damaged Prior to Receipt by User

    IT WAS REPORTED THAT THE CUSTOMER FOUND A 10CH SIZE HYDROSIL GO INTERMITTENT CATHETER IN THE BOX OF 8CH SIZE CATHETER. IT WAS ALSO STATED THAT THE CUSTOMER WILL CALL BACK IF THERE WERE MORE BUT SO FAR IT WAS 1.

    Patient problems: No Known Impact Or Consequence To Patient; No Patient Involvement

    MAUDE report 10554940 ↗

Other CATHETER, STRAIGHT devices

All CATHETER, STRAIGHT devices →

Sources and updates

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